Renan Brandão Rambaldi Cavalheiro

Universidade Federal de São Paulo — Brazil

Neuroscience · Life Sciences

1h-index4citations16works0.32yr avg
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Research Topics

Genetic Neurodegenerative Diseases(2), Heme Oxygenase-1 and Carbon Monoxide(2), Erythrocyte Function and Pathophysiology(2), Neurogenetic and Muscular Disorders Research(2), Porphyrin Metabolism and Disorders(2)

Publications16 total

Arthrogryposis as a neuromuscular phenotype: lessons from <i>PIEZO2</i> loss-of-function
Practical Neurology·2026
Acute Hepatic Porphyria Should Be Included in the Diagnostic Work-Up of Patients with Resistant Hypertension or Suspected Secondary Hypertension
Medical Sciences·2025Open Access
Practical Recommendations in the Treatment of Acute and Chronic Life-Threatening Infectious Diseases in Patients with Acute Hepatic Porphyria
Metabolites·2025· 1 citedOpen Access
Three patients with spinal muscular atrophy who have switched treatments risdiplam following onasemnogene abeparvovec, case report
2025
Distal arthrogryposis with impaired proprioception and touch—A case report
2025
Assessing Chitinases and Neurofilament Light Chain as Biomarkers for Adult-Onset Leukodystrophies
Current Issues in Molecular Biology·2024· 3 citedOpen Access
A diagnostic challenge: is mixed connective tissue disease enough to explain difficult-to-control epilepsy?
Arquivos de Neuro-Psiquiatria·2024Open Access
Challenges in managing acute hepatic porphyrias with comorbid conditions: a case series
Arquivos de Neuro-Psiquiatria·2024Open Access
Case report - ELOVL4: cerebellar ataxia with axonal sensory-motor polyneuropathy, epilepsy, psychosis and cognitive decline
Arquivos de Neuro-Psiquiatria·2024Open Access
Clinical spectrum of the PLA2G6 gene
Arquivos de Neuro-Psiquiatria·2024Open Access
Case report of an autosomal dominant limb-girdle muscular dystrophy due to a heterozygous variant in the CAPN3 gene
Arquivos de Neuro-Psiquiatria·2024Open Access
Clinical and genetic spectrum of the ZFYVE26 gene: an analysis of 7 patients
Arquivos de Neuro-Psiquiatria·2024Open Access
Case report of hematomyelia due to cervical intramedullary cavernous hemangioma after plastic surgery
Arquivos de Neuro-Psiquiatria·2024Open Access
Late-onset biotinidase deficiency mimicking adult leigh syndrome: case report
Arquivos de Neuro-Psiquiatria·2024Open Access
Inborn errors of immunity: neurological phenotypes, clinical features and genetics of a cohort of 27 patients
Arquivos de Neuro-Psiquiatria·2024Open Access
Acquired hemichorea secondary to hyponatremia: a case report
2023Open Access

Frequent Co-authors

Igor Braga Farias(12), João Paulo Barile(12), Paulo Victor Sgobbi de Souza(12), Wladimir Bocca Vieira de Rezende Pinto(11), Paulo de Lima Serrano(10), Patrícia Marques Mendes(9), Kaliny Oliveira Peixoto(9), Acary Souza Bullé Oliveira(9), Daniel Delgado Seneor(7), Ludovic Dumont(3), Rafael Chaves Claudino de Queiroga(3), Patricia Marques Mendes(3), Bruno de Mattos Lombardi Badia(2), Roberta Ismael Lacerda Machado(2), E. Alves Da Silva(2), Caique Veloso(2), Fanny A Garcia(2), Thaiane de Paulo Varollo Rodrigues(1), Leslyê Donato Pinto(1), Indiara Correia Pereira(1)